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Modeling the Embrace of a Mutator: APOBEC Selection of Nucleic Acid Ligands

The 11-member APOBEC (apolipoprotein B mRNA editing catalytic polypeptide-like) family of zinc-dependent cytidine deaminases bind to RNA and single-stranded DNA (ssDNA) and, in specific contexts, modify select (deoxy)cytidines to (deoxy)uridines. In this review, we describe advances made through hig...

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Detalles Bibliográficos
Autores principales: Salter, Jason D., Smith, Harold C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Trends Journals 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6073885/
https://www.ncbi.nlm.nih.gov/pubmed/29803538
http://dx.doi.org/10.1016/j.tibs.2018.04.013
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author Salter, Jason D.
Smith, Harold C.
author_facet Salter, Jason D.
Smith, Harold C.
author_sort Salter, Jason D.
collection PubMed
description The 11-member APOBEC (apolipoprotein B mRNA editing catalytic polypeptide-like) family of zinc-dependent cytidine deaminases bind to RNA and single-stranded DNA (ssDNA) and, in specific contexts, modify select (deoxy)cytidines to (deoxy)uridines. In this review, we describe advances made through high-resolution co-crystal structures of APOBECs bound to mono- or oligonucleotides that reveal potential substrate-specific binding sites at the active site and non-sequence-specific nucleic acid binding sites distal to the active site. We also discuss the effect of APOBEC oligomerization on functionality. Future structural studies will need to address how ssDNA binding away from the active site may enhance catalysis and the mechanism by which RNA binding may modulate catalytic activity on ssDNA.
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spelling pubmed-60738852018-08-09 Modeling the Embrace of a Mutator: APOBEC Selection of Nucleic Acid Ligands Salter, Jason D. Smith, Harold C. Trends Biochem Sci Article The 11-member APOBEC (apolipoprotein B mRNA editing catalytic polypeptide-like) family of zinc-dependent cytidine deaminases bind to RNA and single-stranded DNA (ssDNA) and, in specific contexts, modify select (deoxy)cytidines to (deoxy)uridines. In this review, we describe advances made through high-resolution co-crystal structures of APOBECs bound to mono- or oligonucleotides that reveal potential substrate-specific binding sites at the active site and non-sequence-specific nucleic acid binding sites distal to the active site. We also discuss the effect of APOBEC oligomerization on functionality. Future structural studies will need to address how ssDNA binding away from the active site may enhance catalysis and the mechanism by which RNA binding may modulate catalytic activity on ssDNA. Elsevier Trends Journals 2018-08 /pmc/articles/PMC6073885/ /pubmed/29803538 http://dx.doi.org/10.1016/j.tibs.2018.04.013 Text en © 2018 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Salter, Jason D.
Smith, Harold C.
Modeling the Embrace of a Mutator: APOBEC Selection of Nucleic Acid Ligands
title Modeling the Embrace of a Mutator: APOBEC Selection of Nucleic Acid Ligands
title_full Modeling the Embrace of a Mutator: APOBEC Selection of Nucleic Acid Ligands
title_fullStr Modeling the Embrace of a Mutator: APOBEC Selection of Nucleic Acid Ligands
title_full_unstemmed Modeling the Embrace of a Mutator: APOBEC Selection of Nucleic Acid Ligands
title_short Modeling the Embrace of a Mutator: APOBEC Selection of Nucleic Acid Ligands
title_sort modeling the embrace of a mutator: apobec selection of nucleic acid ligands
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6073885/
https://www.ncbi.nlm.nih.gov/pubmed/29803538
http://dx.doi.org/10.1016/j.tibs.2018.04.013
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